Have questions? Visit https://www.reddit.com/r/SNPedia

rs772551056

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772551056(C;T)
Make rs772551056(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17044824
GeneSDHB
is asnp
is mentioned by
dbSNPrs772551056
ebirs772551056
HLIrs772551056
Exacrs772551056
Varsomers772551056
Maprs772551056
PheGenIrs772551056
hapmaprs772551056
1000 genomesrs772551056
hgdprs772551056
ensemblrs772551056
gopubmedrs772551056
geneviewrs772551056
scholarrs772551056
googlers772551056
pharmgkbrs772551056
gwascentralrs772551056
openSNPrs772551056
23andMers772551056
23andMe allrs772551056
SNP Nexus

SNPshotrs772551056
SNPdbers772551056
MSV3drs772551056
GWAS Ctlgrs772551056
Max Magnitude0
ClinVar
Risk rs772551056(T;T)
Alt rs772551056(T;T)
Reference rs772551056(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome not provided Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed 0
HGVS NC_000001.10:g.17371319C>T
CLNSRC
CLNACC RCV000162578.1, RCV000183217.2, RCV000232432.1,